Medical device licence · 60430 · Class 3
HELIOMOLAR COMPOSITE MATERIALS
No longer licensed: cancelled
Licence status Cancelled; first licensed September 9, 2002; ended November 19, 2024. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 60430
- Licence holder
- Ivoclar Vivadent AgSchaan, Liechtenstein
- Risk class
- Class III (moderate to high risk)
- Licence type
- Device Family
- First licensed
- September 9, 2002
- Ended
- November 19, 2024
- Devices covered
- 5
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- HELIOMOLAR CAVIFIL ASSORTMENT AND REFILLS
- HELIOMOLAR FLOW SYRINGE ASSORTMENT AND REFILLS
- HELIOMOLAR HB CAVIFIL ASSORTMENT AND REFILLS
- HELIOMOLAR HB SYRINGE ASSORTMENT AND REFILLS
- HELIOMOLAR SYRINGE ASSORTMENT AND REFILLS
Recalls and safety alerts that mention it
Health Canada’s recall notices do not carry licence numbers, so these are matched by name: notices whose title or product names “heliomolar”. A notice may cover another product or only some lots: read it to see what it covers.
- Heliomolar Refill (Cavifil)August 15, 2017 · Medical devices · Medical devices · Type III
- Heliomolar Refill (Cavifil)August 14, 2017 · Medical devices · Medical devices · Type III
Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.